Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10231192	1.00[MEX][hapmap]
rs10245486	1.00[MEX][hapmap]
rs11973055	1.00[MEX][hapmap]
rs11976917	1.00[MEX][hapmap]
rs17864959	1.00[ASW][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17865063	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17865133	1.00[YRI][hapmap]
rs17865483	1.00[MEX][hapmap]
rs17865858	0.89[YRI][hapmap]
rs17866780	1.00[YRI][hapmap]
rs17866903	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17866956	1.00[YRI][hapmap]
rs17867020	1.00[YRI][hapmap]
rs17867140	1.00[MEX][hapmap];0.90[MKK][hapmap]
rs17869343	1.00[AMR][1000 genomes]
rs17869367	1.00[MEX][hapmap]
rs17869416	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17875030	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56742208	1.00[AMR][1000 genomes]
rs6948111	1.00[MEX][hapmap]
rs6954791	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs6959432	1.00[YRI][hapmap]
rs6964696	1.00[YRI][hapmap]
rs6976356	1.00[YRI][hapmap]
rs73723522	1.00[AMR][1000 genomes]
rs7786082	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831121	chr7:126593363-126774413	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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